Verloes A - Search Results

1

Molecular analysis of pericentrin gene (PCNT) in a series of 24 Seckel/microcephalic osteodysplastic primordial dwarfism type II (MOPD II) families.

Willems M, Geneviève D, Borck G, Baumann C, Baujat G, Bieth E, Edery P, Farra C, Gerard M, Héron D, Leheup B, Le Merrer M, Lyonnet S, Martin-Coignard D, Mathieu M, Thauvin-Robinet C, Verloes A, Colleaux L, Munnich A, Cormier-Daire V. Willems M, et al. Among authors: verloes a. J Med Genet. 2010 Dec;47(12):797-802. doi: 10.1136/jmg.2009.067298. Epub 2009 Jul 29. J Med Genet. 2010. PMID: 19643772 Free article.

2

The orocraniodigital syndrome of Juberg and Hayward.

Verloes A, Le Merrer M, Davin JC, Wittamer P, Abrassart C, Bricteux G, Briard ML. Verloes A, et al. J Med Genet. 1992 Apr;29(4):262-5. doi: 10.1136/jmg.29.4.262. J Med Genet. 1992. PMID: 1583649 Free PMC article. Review.

3

Lumping of CFC and Baraitser-Patton Noonan-like syndromes.

Verloes A, Le Merrer M. Verloes A, et al. Am J Med Genet. 1992 Mar 1;42(5):756-7. doi: 10.1002/ajmg.1320420529. Am J Med Genet. 1992. PMID: 1632454 No abstract available.

4

Metaphyseal acroscyphodysplasia.

Verloes A, Le Merrer M, Farriaux JP, Maroteaux P. Verloes A, et al. Clin Genet. 1991 May;39(5):362-9. doi: 10.1111/j.1399-0004.1991.tb03043.x. Clin Genet. 1991. PMID: 1860252

5

Holoprosencephaly-polydactyly ('pseudotrisomy 13') syndrome: a syndrome with features of hydrolethalus and Smith-Lemli-Opitz syndromes. A collaborative multicentre study.

Verloes A, Aymé S, Gambarelli D, Gonzales M, Le Merrer M, Mulliez N, Philip N, Roume J. Verloes A, et al. J Med Genet. 1991 May;28(5):297-303. doi: 10.1136/jmg.28.5.297. J Med Genet. 1991. PMID: 1865466 Free PMC article. Review.

6

Recessive metaphyseal dysplasia without hypotrichosis. A syndrome clinically distinct from McKusick cartilage-hair hypoplasia.

Verloes A, Pierard GE, Le Merrer M, Maroteaux P. Verloes A, et al. J Med Genet. 1990 Nov;27(11):693-6. doi: 10.1136/jmg.27.11.693. J Med Genet. 1990. PMID: 2277385 Free PMC article.

7

BBBG syndrome or Opitz syndrome: new family.

Verloes A, Le Merrer M, Briard ML. Verloes A, et al. Am J Med Genet. 1989 Nov;34(3):313-6. doi: 10.1002/ajmg.1320340303. Am J Med Genet. 1989. PMID: 2688419 Review.

8

[Variable expression of an autosomal dominant syndrome: (BBB syndrome or G syndrome)].

Le Merrer M, Verloes A, Narcy P, Briard ML. Le Merrer M, et al. Among authors: verloes a. J Genet Hum. 1988 Jun;36(3):257-64. J Genet Hum. 1988. PMID: 3411306 French.

9

Microcephalic osteodysplastic dwarfism (type II-like) in siblings.

Verloes A, Lambrechts L, Senterre J, Lambotte C. Verloes A, et al. Clin Genet. 1987 Aug;32(2):88-94. doi: 10.1111/j.1399-0004.1987.tb03331.x. Clin Genet. 1987. PMID: 3652495

10

Heterogeneity of SPONASTRIME dysplasia: delineation of a variant form with severe mental retardation.

Verloes A, Misson JP, Dubru JM, Jamblin P, Le Merrer M. Verloes A, et al. Clin Dysmorphol. 1995 Jul;4(3):208-15. Clin Dysmorphol. 1995. PMID: 7551156

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